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At least 361 records · Page 20Linked to original sources
USGS2000

Analysis of water-quality trends at two discharge stations — One within Big Cypress National Preserve and one near Biscayne Bay — Southern Florida, 1966-94

An analysis of water-quality trends was made at two U.S. Geological Survey daily discharge stations in southern Florida. The ESTREND computer program was the principal tool used for the determination of water-quality trends at the Miami Canal station west of Biscayne Bay in Miami and the Tamiami Canal station along U.S. Highway 41 in the Big Cypress National Preserve in Collier County. Variability in water quality caused by both seasonality and streamflow was compensated for by applying the nonparametric Seasonal Kendall trend test to unadjusted concentrations or flow-adjusted concentrations (residuals) determined from linear regression analysis. Concentrations of selected major inorganic constituents and physical characteristics; pH and dissolved oxygen; suspended sediment; nitrogen, phosphorus, and carbon species; trace metals; and bacteriological and biological characteristics were determined at the Miami and Tamiami Canal stations. Median and maximum concentrations of selected constituents were compared to the Florida Class III freshwater standards for recreation, propagation, and maintenance of a healthy, well-balanced population of fish and wildlife. The median concentrations of the water-quality constituents and characteristics generally were higher at the Miami Canal station than at the Tamiami Canal station. The maximum value for specific conductance at the Miami Canal station exceeded the State standard. The median and maximum concentrations for ammonia at the Miami and Tamiami Canal stations exceeded the State standard, whereas median dissolved-oxygen concentrations at both stations were below the State standard. Trend results were indicative of either improvement or deterioration in water quality with time. Improvement in water quality at the Miami Canal station was reflected by downward trends in suspended sediment (1987-94), turbidity, (1970-78), total ammonia (1971-94), total phosphorus (1987-94), barium (1978-94), iron (1969-94), and fecal coliform (1976-94). Deterioration in water quality at the same station was indicated by upward trends in specific conductance (1966-94), dissolved solids (1966-94, 1976-94, and 1987-94), chloride (1966-94), potassium (1966-94), magnesium (1966-94), sodium (1966-94), sulfate (1966-94), silica (1966-94), suspended sediment (1974-94), total organic carbon (1970-81), and fecal streptococcus (1987-94). The downward trend in pH (1966-94) was indicative of deterioration in water quality at the Miami Canal station. Improvement in water quality at the Tamiami Canal station was reflected by downward trends in fluoride (1967-93), total ammonia (1970-92), total nitrite plus nitrate (1975-85), and barium (1978-93). Deterioration in water quality at the same station was statistically significant by upward trends in specific conductance (1967-93), dissolved solids (1967-93), chloride (1967-93), sodium (1967-93), potassium (1967-93), magnesium (1967-93), strontium (1967-93), and suspended sediment (1976-93). The downward trend in dissolved oxygen (1970-93) was indicative of deterioration in water quality.

Florida↗
USGS2000

Ground-water quality in alluvial aquifers in the eastern Iowa basins, Iowa and Minnesota

The quality of shallow alluvial ground water that is used for domestic supplies in the Wapsipinicon, Cedar, Iowa, and Skunk River Basins (Eastern Iowa Basins) is described. Water samples from 32 domestic-supply wells were collected from June through July 1998. This study of ground-water quality in alluvial aquifers in the Eastern Iowa Basins is part of the U.S. Geological Survey's National Water-Quality Assessment Program. Calcium and bicarbonate were the dominant ions in solution, likely derived from the dissolution of carbonate minerals in the alluvial aquifer material. Concentrations of iron exceeded the U.S. Environmental Protection Agency Secondary Maximum Contaminant Level (300 micrograms per liter) for drinking water in 53 percent of the samples, and 50 percent of the samples exceeded the Secondary Maximum Contaminant Level for manganese (50 micrograms per liter). pH and alkalinity increased and sulfate concentrations decreased with increasing well depth. Nitrite plus nitrate nitrogen was detected in 53 percent of the samples and exceeded the U.S. Environmental Protection Agency Maximum Contaminant Level of 10 milligrams per liter for drinking water in 13 percent of the samples. Nitrite plus nitrate nitrogen concentrations were negatively correlated with well depth and positively correlated with percentage of oxygen saturation. Ammonia plus organic nitrogen concentrations were positively correlated with well depth, and ratios of nitrite plus nitrate to ammonia were positively correlated with percentage of oxygen saturation. The majority of samples, 72 percent, contained water recharged since the early 1950's. The recharge date of water was earlier in deeper wells. Nitrite plus nitrate and total pesticide concentrations were greater in more recently recharged water. Eight pesticides and eight pesticide metabolites were detected in ground-water samples. Atrazine was the most commonly detected pesticide, and metolachlor ethanesulfonic acid was the most commonly detected metabolite. No pesticide detections exceeded U.S. Environmental Protection Agency drinking-water Maximum Contaminant Levels. The effects of land use on ground-water quality also were examined. There was a positive correlation between percentage of land used for soybean production and concentrations of metolachlor, metolachlor ethanesulfonic acid, and metolachlor oxanilic acid in ground-water samples. Data from this study and from previous studies in the Eastern Iowa Basins were compared statistically by well type (domestic, municipal, and monitoring wells). Well depths were significantly greater in domestic and municipal wells than in monitoring wells. pH, calcium, sulfate, chloride, and atrazine concentrations were significantly higher in municipal-well samples than in domestic-well samples. pH and sulfate concentrations were significantly higher in municipal-well samples than in monitoring-well samples. Ammonia was significantly higher in domestic-well samples than in monitoring-well samples, chloride was significantly higher in monitoring-well samples than in domestic-well samples, and fluoride was significantly higher in domestic-well samples than in municipal-well samples.

Iowa, Minnesota↗
USGS2000

Ground-water quality atlas of Oakland County, Michigan

The U.S. Geological Survey (USGS), in cooperation with Oakland County Health Division (OCHD), collected 140 water samples from 38 wells in Oakland County during 1998 to better understand ground-water quality. OCHD had observed temporal variations in concentrations of various constituents, so two additional sets of samples were collected to evaluate potential short-term variability related to sample collection procedures and long-term seasonal variability. Replicate samples from 28 wells were analyzed in the Michigan Department of Environmental Quality (MDEQ) Drinking Water Laboratory to compare MDEQ’s analytical results to those obtained from the USGS National Water Quality Laboratory. Several additional databases describing population, land use, water supply, soils, geology, and flows of ground water and surface water are presented in the first part of the report to assist in interpreting the water-quality data. Maps created from these databases are provided in the first portion of the report as an extension of the study-area description. The U.S. Environmental Protection Agency (USEPA) has established Maximum Contaminant Levels (MCL) and Secondary Maximum Contaminant Levels (SMCL) for which samples were analyzed in this study. Water from the 38 wells sampled by the USGS did not exceed the SMCL or MCL for sulfate, fluoride, or nitrite. However, water from 26 wells exceeded the SMCL for iron, water from 12 wells exceeded the SMCL for manganese, and water from 12 wells exceeded the SMCL for dissolved solids. Water from two wells exceeded the MCL for nitrate, although nitrate concentrations in water from most wells was below the detection limit. Water from seven wells exceeded the SMCL for chloride, and water from all wells contained detectable concentrations of chloride. Water from five wells exceeded the MCL for arsenic, and most of the wells sampled contained detectable concentrations of arsenic. These five wells were identified from previous MDEQ analyses to have elevated arsenic concentrations, and were sampled to obtain additional chemistry information. Replicate samples were collected from 26 of the 38 wells for analysis at the MDEQ Drinking-Water Laboratory to compare the results with the USGS National Water Quality Laboratory. The results of the replicate analyses indicate close agreement between the laboratories, with mean differences for nitrate, chloride, and arsenic of 0.10 milligrams per liter (mg/L) as nitrogen, 6.8 mg/L, and 0.0008 mg/L, respectively between the USGS and MDEQ analyses. Potential health effects associated with ingesting nitrate, chloride, and arsenic are provided with the water-quality data, along with references for further information.

Michigan↗
USGS2001

Ground-water quality, levels, and flow direction near Fort Cobb Reservoir, Caddo County, Oklahoma, 1998-2000

Fort Cobb Reservoir in northwest Caddo County Oklahoma is managed by the Bureau of Reclamation for water supply, recreation, flood control, and wildlife. Excessive amounts of nitrogen in the watershed have the potential to cause long-term eutrophication of the reservoir and increase already elevated concentrations of nitrogen in the Rush Springs aquifer. The U.S. Geological Survey in cooperation with the Bureau of Reclamation studied ground water in the area surrounding a swine feeding operation located less than 2 miles upgradient from Fort Cobb Reservoir in Caddo County, Oklahoma. Objectives of the study were to (1) determine if the operation was contributing nitrogen to the ground water and (2) measure changes in ground-water levels and determine the local ground-water flow direction in the area surrounding the swine feeding operation. Nitrate concentrations (28.1 and 31.5 milligrams per liter) were largest in two ground-water samples from a well upgradient of the wastewater lagoon. Nitrate concentrations ranged from 4.30 to 8.20 milligrams per liter in samples from downgradient wells. Traces of ammonia and nitrite were detected in a downgradient well, but not in upgradient wells. d15N values indicate atmospheric nitrogen, synthetic fertilizer, or plants were the predominate sources of nitrate in ground water from the downgradient wells. The d15N values in these samples are depleted in nitrogen-15, indicating that animal waste was not a significant contributor of nitrate. Manganese concentrations (1,150 and 965 micrograms per liter) in samples from a downgradient well were substantially larger than concentrations in samples from other wells, exceeding the secondary drinking-water standard of 50 micrograms per liter. Larger concentrations of bicarbonate, magnesium, fluoride, and iron and a higher pH were also measured in water from a downgradient well. Ground-water levels in an observation well were higher from April to mid-July and lower during the late summer and in the fall due to a seasonal decrease in precipitation, increase in water withdrawals, and increase in evapotranspiration. Ground water near the wastewater spray field moved south-southeast toward Willow Creek along a gradient of about 50 feet per mile. Analysis of ground-water samples suggest that commercial fertilizer is contributing nitrate upgradient of the swine feeding operation and that wastewater from the lagoon is contributing reduced forms of nitrogen, ammonia and nitrite. Additional downgradient wells would be needed to (1) determine if the swine feeding operation is adding excessive amounts of nitrogen to ground water, (2) determine the vertical dimension of wastewater flow, and (3) the extent of wastewater downgradient of the lagoon.

Water-Resources Investigations Report↗
USGS2001

Geochemistry and origins of mineralized waters in the Floridan aquifer system, northeastern Florida

Increases in chloride concentration have been observed in water from numerous wells tapping the Floridan aquifer system in northeastern Florida. Although most increases have been in the eastern part of Duval County, Florida, no spatial pattern in elevated chloride concentrations is discernible. Possible sources of the mineralized water include modern seawater intrusion; unflushed Miocene-to-Pleistocene-age seawater or connate water in aquifer sediments; or mineralized water from deeper zones of the aquifer system or from formations beneath the Floridan aquifer system. The purpose of this study was to document the chemical and isotopic characteristics of water samples from various aquifer zones, and from geochemical and hydrogeologic data, to infer the source of the increased mineralization. Water samples were collected from 53 wells in northeastern Florida during 1997-1999. Wells tapped various zones of the aquifer including: the Fernandina permeable zone (FPZ), the upper zone of the Lower Floridan aquifer (UZLF), the Upper Floridan aquifer (UFA), and both the UFA and the UZLF. Water samples were analyzed for major ions and trace constituents and for isotopes of carbon, oxygen, hydrogen, sulfur, strontium, chlorine, and boron. Samples of rock from the aquifer were analyzed for isotopes of oxygen, carbon, and strontium. In general, water from various aquifer zones cannot be differentiated based on chemistry, except for water from FPZ wells. Major-ion concentrations vary as much within the upper zone of the Lower Floridan aquifer and the Upper Floridan aquifer as between these two zones. Simple models of mixing between fresh ground water and either modern seawater or water from the FPZ as a mineralized end member show that many water samples from the UZLF aquifer and the UFA are enriched in bicarbonate, calcium, magnesium, sulfate, fluoride, and silica and are depleted in sodium and potassium (as compared to concentrations predicted by simple mixing). Chemical mass-balance models of mixing and reactions between a hypothetical initial seawater and aquifer minerals cannot account for the observed water chemistry in a few wells, implying a source other than seawater, either ancient or modern, or the occurrence of other more complex rock-water reactions. Hydrogeologic and geochemical data from water and aquifer samples indicate that the most likely source of mineralized water in some wells yielding water with increasing chloride concentrations is water from the FPZ. In other wells, the flushing of Miocene-to-Pleistocene-age seawater can account for the observed chloride concentrations. The fact that most of the water samples collected are a mixture of less than one percent of mineralized water with more than 99 percent fresh or recharge water makes identifying the source of the mineralized water difficult. Differences in carbon-14 and sulfur-34 values probably reflect areal differences in aquifer mineralogy and distribution of organic carbon related to paleokarst features. Geochemical mass-balance models of seawater-rock interaction are unable to account for the chemical and isotopic composition of mineralized water from the FPZ, which implies another source of mineralized water, such as a brine, or the occurrence of more complex water-rock reactions.

Water-Resources Investigations Report↗
USGS2001

Characterization of surface-water quality based on real-time monitoring and regression analysis, Quivira National Wildlife Refuge, south-central Kansas, December 1998 through June 2001

Because of the considerable wildlife benefits offered by the Quivira National Wildlife Refuge in south-central Kansas, there is a desire to ensure suitable water quality. To assess the quality of water flowing from Rattlesnake Creek into the refuge, the U.S. Geological Survey collected periodic water samples from December 1998 through June 2001 and analyzed the samples for physical properties, dissolved solids, total suspended solids, suspended sediment, major ions, nutrients, metals, pesticides, and indicator bacteria. Concentrations of 10 of the 125 chemicals analyzed did not meet water-quality criteria to protect aquatic life and drinking water in a least one sample. These were pH, turbidity, dissolved oxygen, dissolved solids, sodium, chloride, phosphorus, total coliform bacteria, E. coli bacteria, and fecal coliform bacteria. No metal or pesticide concentrations exceeded water-quality criteria. Twenty-two of the 43 metals analyzed were not detected, and 36 of the 46 pesticides analyzed were not detected. Because dissolved solids, sodium, chloride, fecal coliform bacteria, and other chemicals that are a concern for the health and habitat of fish and wildlife at the refuge cannot be measured continuously, regression equations were developed from a comparison of the analytical results of periodic samples and in-stream monitor measurements of specific conductance, pH, water temperature, turbidity, and dissolved oxygen. A continuous record of estimated chemical concentrations was developed from continuously recorded in-stream measurements. Annual variation in water quality was evaluated by comparing 1999 and 2000 sample data- the 2 years for which complete data sets were available. Median concentrations of alkalinity, fluoride, nitrate, and fecal coliform bacteria were smaller or did not change from 1999 to 2000. Dissolved solids, total suspended solids, sodium, chloride, sulfate, total organic nitrogen, and total phosphorus had increases in median concentrations from 1999 to 2000. Increases in the median concentrations of the major ions were expected due to decreased rainfall in 2000 and very low streamflow late in the year. Increases for solids and nutrients may have been due to the unusually high streamflow in the early spring of 2000. This was the time of year when fields were tilled, exposing solids and nutrients that were transported with runoff to Rattlesnake Creek. Load estimates indicate the chemical mass transported into the refuge and can be used in the development of total maximum daily loads (as specified by the U.S. Environmental Protection Agency) for water-quality contaminants in Rattlesnake Creek. Load estimates also were used to evaluate seasonal variation in water quality. Seasonal variation was most pronounced in the estimates of nutrient loads, and most of the nutrient load transported to the refuge occurred during just a few periods of surface runoff in the spring and summer. This information may be used by resource managers to determine when water-diversion strategies would be most beneficial. Load estimates also were used to calculate yields, which are useful for site comparisons. The continuous and real-time nature of the record of estimated concentrations, loads, and yields may be important for resource managers, recreationalists, or others for evaluating water-diversion strategies, making water-use decisions, or assessing the environmental effects of chemicals in time to prevent adverse effects on fish or other aquatic life at the refuge.

Kansas↗
USGS2002

Water quality and aquatic communities of upland wetlands, Cumberland Island National Seashore, Georgia, April 1999 to July 2000

Cumberland Island is the southernmost and largest barrier island along the coast of Georgia. The island contains about 2,500 acres of freshwater wetlands that are located in a variety of physical settings, have a wide range of hydroperiods, and are influenced to varying degrees by surface and ground water, rainwater, and seawater. In 1999-2000, the U.S. Geological Survey, in cooperation with the National Park Service, conducted a water-quality study of Cumberland Island National Seashore to document and interpret the quality of a representative subset of surface- and ground-water resources for management of the seashore's natural resources. As part of this study, historical ground-water, surface-water, and ecological studies conducted on Cumberland Island also were summarized. Surface-water samples from six wetland areas located in the upland area of Cumberland Island were collected quarterly from April 1999 to March 2000 and analyzed for major ions, nutrients, trace elements, and field water-quality constituents including specific conductance, pH, temperature, dissolved oxygen, alkalinity, tannin and lignin, and turbidity. In addition, water temperature and specific conductance were recorded continuously from two wetland areas located near the mean high-tide mark on the Atlantic Ocean beaches from April 1999 to July 2000. Fish and invertebrate communities from six wetlands were sampled during April and December 1999. The microbial quality of the near-shore Atlantic Ocean was assessed in seawater samples collected for 5 consecutive days in April 1999 at five beaches near campgrounds where most recreational water contact occurs. Ground-water samples were collected from the Upper Floridan aquifer in April 1999 and from the surficial aquifer in April 2000 at 11 permanent wells and 4 temporary wells (drive points), and were analyzed for major ions, nutrients, trace elements, and field water-quality constituents (conductivity, pH, temperature, dissolved oxygen, and alkalinity). Fecal-coliform bacteria concentrations were measured, but not detected, in samples collected from two domestic water-supply wells. During the 12-month period from April 1999 to March 2000 when water-quality and aquatic-community samples were collected, rainfall was 12.93 inches below the 30-year average rainfall. Constituent concentrations were highly variable among the different wetlands during the study period. Rainfall and tidal surges associated with tropical storms and hurricanes substantially influenced water quantity and quality, particularly in wetland areas directly influenced by tidal surges. Although surface waters on Cumberland Island are not used as sources of drinking water, exceedances of U.S. Environmental Protection Agency primary and secondary standards for drinking water were noted for comparative purposes. A nitrate concentration of 12 milligrams per liter in one sample from Whitney outflow was the only exceedance of a maximum contaminant level. Secondary standards were exceeded in 26 surface-water samples for the following constituents: pH (10 exceedances), chloride (8), sulfate (5), total dissolved solids (4), iron (2), fluoride (1), and manganese (1). The total-dissolved-solids concentrations and the relative abundance of major ions in surface-water samples collected from wetlands on Cumberland Island provide some insight into potential sources of water and influences on water quality. Major-ion chemistries of water samples from Whitney Lake, Willow Pond, and South End Pond 3 were sodium-chloride dominated, indicating direct influence from rainwater, salt aerosol, or inundation of marine waters. The remaining wetlands sampled had low total-dissolved-solids concentrations and mixed major-ion chemistries--North Cut Pond 2A was magnesium-sodium-chloride-sulfate dominated and Lake Retta and the two beach outflows were sodium-calcium-bicarbonate-chloride dominated. The higher percent calcium and bicarbonate in some wetlands sugg

Georgia↗
USGS2002

Statistical analysis of stream water-quality data and sampling network design near Oklahoma City, central Oklahoma, 1977-1999

Water-quality data collected from 1993-99 at five sites on Bluff, Deer, and Chisholm Creeks and from 1988-99 at five sites in the North Canadian River indicated that there were significant differences in constituent values among sites for water properties, major ions, trace elements, nutrients, turbidity, pesticides, and bacteria. Concentrations of dissolved solids and sulfate generally decreased as streams flowed through the Oklahoma City urban area. Concentrations of organic carbon, nitrogen and phosphorus compounds, lindane, and 2,4-D, and frequencies of detection of pesticides increased in the North Canadian River as it flowed through the urban area. Volatile organic compounds were not detected in samples collected quarterly from 1988-90 at sites on the North Canadian River. Concentrations of some compounds, including dissolved oxygen, sulfate, chloride, ammonia, manganese, diazinon, dieldrin, and fecal coliform bacteria periodically exceeded Federal or state water-quality standards at some sites. Regression analyses were used to identify trends in constituent concentrations related to streamflow, season, and time. Trends for some constituents were indicated at all sites, but most trends were sitespecific. Seasonal trends were evident for several constituents: suspended solids, organic nitrogen, and biochemical oxygen demand were greatest during summer. Dissolved oxygen, ammonia, and nitrite plus nitrate-nitrogen were greatest during winter. Concentrations of dissolved oxygen, fluoride, sulfate, total suspended solids, iron, and manganese generally increased with time. Concentrations of chloride, nitrite plus nitrate-nitrogen, dissolved phosphorus, dissolved orthophosphate, biochemical oxygen demand, dieldrin, and lindane decreased with time. There was relatively little change in land use from the late 1970s to the mid-1990s due to relatively modest rates of population growth in the study area during that period. Most changes in water quality in these streams and rivers may be due to changes in chemical use and wastewater treatment practices. The sampling network was evaluated with respect to areal coverage, sampling frequency, and analytical schedules. Areal coverage could be expanded to include one additional watershed that is not part of the current network. A new sampling site on the North Canadian River might be useful because of expanding urbanization west of the city, but sampling at some other sites could be discontinued or reduced based on comparisons of data between the sites. Additional real-time or periodic monitoring for dissolved oxygen may be useful to prevent anoxic conditions in pools behind new low-water dams. The sampling schedules, both monthly and quarterly, are adequate to evaluate trends, but additional sampling during flow extremes may be needed to quantify loads and evaluate water-quality during flow extremes. Emerging water-quality issues may require sampling for volatile organic compounds, sulfide, total phosphorus, chlorophyll- a , Esherichia coli , and enterococci, as well as use of more sensitive laboratory analytical methods for determination of cadmium, mercury, lead, and silver.

Oklahoma↗
USGS2002

Ground-water flow simulation and chemical and isotopic mixing equation analysis to determine source contributions to the Missouri River alluvial aquifer in the vicinity of the Independence, Missouri, well field

The city of Independence, Missouri, operates a well field in the Missouri River alluvial aquifer. Steady-state ground-water flow simulation, particle tracking, and the use of chemical and isotopic composition of river water, ground water, and well-field pumpage in a two-component mixing equation were used to determine the source contributions of induced inflow from the Missouri River and recharge to ground water from precipitation in well-field pumpage. Steady-state flow-budget analysis for the simulation-defined zone of contribution to the Independence well field indicates that 86.7 percent of well-field pumpage is from induced inflow from the river, and 6.7 percent is from ground-water recharge from precipitation. The 6.6 percent of flow from outside the simulation-defined zone of contribution is a measure of the uncertainty of the estimation, and occurs because model cells are too large to uniquely define the actual zone of contribution. Flow-budget calculations indicate that the largest source of water to most wells is the Missouri River. Particle-tracking techniques indicate that the Missouri River supplies 82.3 percent of the water to the Independence well field, ground-water recharge from precipitation supplies 9.7 percent, and flow from outside defined zones of contribution supplies 8.0 percent. Particle tracking was used to determine the relative amounts of source water to total well-field pumpage as a function of traveltime from the source. Well-field pumpage that traveled 1 year or less from the source was 8.8 percent, with 0.6 percent from the Missouri River, none from precipitation, and 8.2 percent between starting cells. Well-field pumpage that traveled 2 years or less from the source was 10.3 percent, with 1.8 percent from the Missouri River, 0.2 percent from precipitation, and 8.3 percent between starting cells. Well-field pumpage that traveled 5 years or less from the source was 36.5 percent, with 27.1 percent from the Missouri River, 1.1 percent from precipitation, and 8.3 percent between starting cells. Well-field pumpage that traveled 10 years or less from the source was 42.7 percent, with 32.6 percent from the Missouri River, 1.8 percent from precipitation, and 8.3 percent between starting cells. Well-field pumpage that traveled 25 years or less from the source was 71.9 percent, with 58.9 percent from the Missouri River, 4.7 percent from precipitation, and 8.3 percent between starting cells. Results of chemical (calcium, sodium, iron, and fluoride) and isotopic (oxygen and hydrogen) analyses of water samples collected from the Missouri River, selected monitoring wells around the Independence well field, and combined well-field pumpage were used in a two component mixing equation to estimate the relative amount of Missouri River water in total well-field pumpage. The relative amounts of induced inflow from the Missouri River in well-field pumpage ranged from 49 percent for sodium to 80 percent for calcium, and sensitivities ranged from 0 percent for iron to plus or minus 35 percent for naturally occurring stable isotope ( 18 O). The average of all mixing equation results indicated that 61 percent of well-field pumpage was from induced inflow from the Missouri River. All methods used in the study indicate that more than one-half of the water in well-field pumpage was inflow from the Missouri River. River inflow estimates from ground-water simulation methods are larger and error values are smaller than those using chemical and isotopic data in the mixing equation, although substantial uncertainties exist for both estimation methods. Because of the complex hydrology of the aquifer near the Independence well field, the source estimates using particle tracking probably are the most reliable of the ground-water simulation methods. Mixing equation results are less reliable than those of the ground-water simulation for this study. However, more reliable results can be obtained from the mixing equation by increasing the number of samples and collecting samples for a longer period of time, and during different flow conditions. In the absence of a calibrated ground-water flow simulation, the mixing equation can provide a reasonable estimate of the sources of water to a well field at relatively low cost, if sources of error are clearly understood.

Water-Resources Investigations Report↗
USGS2003

Arsenic in midwestern glacial deposits — Occurrence and relation to selected hydrogeologic and geochemical factors

Ground-water-quality data collected as part of 12 U.S. Geological Survey National Water-Quality Assessment studies during 1996-2001 were analyzed to (1) document arsenic occurrence in four types of gla-cial deposits that occur in large areas of the Midwest, (2) identify hydrogeologic or geochemical factors asso-ciated with elevated arsenic concentrations, and (3) search for clues as to arsenic source(s) or mechanism(s) of mobilization that could be useful for designing future studies. Arsenic and other water-quality constituents were sampled in 342 monitor and domestic wells in parts of Illinois Indiana Ohio Michigan and Wisconsin. Arsenic was detected (at a concentration >1 ?g/L) in one-third of the samples. The maximum concentration was 84 ?g/L, and the median was less than 1 ?g/L. Eight percent of samples had arsenic concentrations that exceeded the U.S. Environmental Protection Agency Maximum Contaminant Level (MCL) of 10?g/L. Samples were from four aquifer types?confined valley fill, unconfined valley fill, outwash plain, and till with sand lenses. Highest arsenic concentrations were found in reducing waters from valley-fill depos-its. In confined valley fill, all waters were reducing and old (recharged before 1953), and almost half of sam-ples had arsenic concentrations greater than the MCL. In unconfined valley fill, redox conditions and ages were varied, and elevated arsenic concentrations were sporadic. In both types of valley fill, elevated arsenic concentrations are linked to the underlying bedrock on the basis of spatial relations and geochemical correla-tions. In shallow (<50 ft) till with sand lenses, arsenic was detected in oxic or mixed waters, but concentra-tions were rarely greater than the MCL. In shallow out-wash-plain deposits, arsenic concentrations greater than the MCL were detected in waters that were reduc-ing and young (recharged after 1953). Although arsenic concentrations were signifi-cantly higher in deep wells (>150 ft), all deep wells were from a distinctive aquifer type (confined valley fill). It is not known whether wells at similar depths in other aquifer types would produce waters with simi-larly high arsenic concentrations. Correlations of arsenic with fluoride, strontium, and barium suggest that arsenic might be related to epi-genetic (Mississippi Valley-type) sulfide deposits in Paleozoic bedrock. Arsenic is typically released from sulfides by oxidation, but in the current study, the highest arsenic concentrations in glacial deposits were detected in reducing waters. Therefore, a link between epigenetic sulfides and elevated arsenic concentrations in glacial deposits would probably require a multi-step process.

Illinois, Indiana, Ohio↗
USGS2004

Water-quality characteristics and ground water quantity of the Fraser River watershed, Grand County, Colorado, 1998-2001

The U.S. Geological Survey, in cooperation with the Grand County Board of County Commissioners, conducted a 4-year study to assess ground- and surface-water-quality conditions and ground-water quantity in the 302-square-mile Fraser River watershed in north-central Colorado. The Fraser River flows north about 28 miles from the headwaters near the Continental Divide, through the towns of Winter Park, Fraser, Tabernash, and Granby, and is one of the major tributaries to the Upper Colorado River. Increasing urban development, as well as the seasonal influx of tourists, is placing more demands on the water resources in the Fraser River watershed. A ground-water sampling network of 11 wells was established to represent different aquifer systems (alluvial, Troublesome Formation, Precambrian granite), land uses (urban, nonurban), and areas with or without individual septic disposal system use. The well network was sampled for ground-water quality on a semiannual basis from August 1998 through September 2001. The sampling included field properties and the collection of water samples for analysis of major ions, trace elements, nutrients, dissolved organic carbon, bacteria, methylene blue active substances, and radon-222. One surface-water site, on the Fraser River just downstream from the town of Tabernash, Colorado, was sampled bimonthly from August 1998 through September 2001 to assess the cumulative effects of natural and human processes on water quality in the upper part of the Fraser River watershed. Surface-water-quality sampling included field properties and the collection of water-quality samples for analysis of major ions, trace elements, nutrients, organic carbon, and bacteria. Ground water was a calcium-bicarbonate type water and is suitable as a drinking-water, domestic, municipal, industrial, and irrigation source. In general, no widespread ground-water-quality problems were indicated. All pH values and concentrations of dissolved solids, chloride, fluoride, sulfate, nitrite, and nitrate in the ground-water samples met or were substantially less than U.S. Environmental Protection Agency drinking-water standards and health advisories or State of Colorado water-quality standards. Federal standards for turbidity and concentrations of iron, manganese, methylene blue active substances, and radon-222 were not met in water samples from at least one well. The only ground-water-quality concern assessed by this study is radon-222, which was detected in all radon- analyzed samples from 10 wells at levels exceeding the proposed U.S. Environmental Protection Agency drinking-water standard of 300 picocuries per liter. Concentrations of chloride, magnesium, and sulfate were statistically different (higher) in ground-water samples from wells completed in the alluvial aquifer, urbanized areas, and areas with individual septic disposal system use than those from wells completed in the Troublesome Formation, nonurban areas, and areas without individual septic disposal system use. Dissolved organic carbon concentrations were statistically higher in ground-water samples from wells completed in the alluvial aquifer and areas without individual septic disposal system use than those from wells completed in the Troublesome Formation and areas with individual septic disposal system use. Differences in dissolved organic-carbon concentrations between the latter category and areas without septic systems likely had no environmental significance. Surface water at the site Fraser River below Crooked Creek at Tabernash was a calcium-bicarbonate type water and is suitable as a drinking-water, residential, commercial, and irrigation resource. All pH values and concentrations of dissolved oxygen were within the State of Colorado instream water-quality standards, and all concentrations of chloride, sulfate, iron, manganese, un-ionized ammonia, nitrite, nitrate, and fecal coliform bacteria met State standards. Seasonal changes in the values or conc

Colorado↗
USGS2004

Reconnaissance of chemical and biological quality in the Owyhee River from the Oregon State line to the Owyhee Reservoir, Oregon, 2001&ndash;02

The Owyhee River drains an extremely rugged and sparsely populated landscape in northern Nevada, southwestern Idaho, and eastern Oregon. Most of the segment between the Oregon State line and Lake Owyhee is part of the National Wild and Scenic Rivers System, and few water-quality data exist for evaluating environmental impacts. As a result, the U.S. Geological Survey, in cooperation with the Bureau of Land Management, assessed this river segment to characterize chemical and biological quality of the river, identify where designated beneficial uses are met and where changes in stream quality occur, and provide data needed to address activities related to environmental impact assessments and Total Maximum Daily Loads. Water-quality issues identified at one or more sites were water temperature, suspended sediment, dissolved oxygen, pH, nutrients, trace elements, fecal bacteria, benthic invertebrate communities, and periphyton communities. Generally, summer water temperatures routinely exceeded Oregon's maximum 7-day average criteria of 17.8 degrees Celsius. The presence of few coldwater taxa in benthic invertebrate communities supports this observation. Suspended-sediment concentrations during summer base flow were less than 10 milligrams per liter (mg/L). Dissolved solids concentrations ranged from 46 to 222 mg/L, were highest during base flow, and tended to increase in a downstream direction. Chemical compositions of water samples indicated that large proportions of upland-derived water extend to the lower reaches of the study area during spring runoff. Dissolved fluoride and arsenic concentrations were highest during base flow and may be a result of geothermal springs discharging to the river. No dissolved selenium was detected. Upstream from the Rome area, spring runoff concentrations of suspended sediment ranged from 0 to 52 mg/L, and all except at the Three Forks site were typically below 20 mg/L. Stream-bottom materials from the North Fork Owyhee River, an area with no mines, were enriched with nine trace elements, which indicates that this basin may be a natural source of these elements. Near Rome, the part of the study area not included in the National Wild and Scenic Rivers System, land-use impacts resulted in elevated populations of Escherichia coli bacteria ( E. coli ) during base flow and elevated concentrations of nitrogen and phosphorus during spring runoff. Sites in this area had the highest numbers of benthic invertebrates; the fewest Ephemeroptera, Plecoptera, and Trichoptera taxa; and the highest Hilsenhoff Biotic Index scores. These results suggest degraded stream quality. Periphyton communities at sites in this area approached nuisance levels and could cause significant dissolved oxygen depletions and pH values that exceed Oregon's recommended criteria. Stream-bottom materials from Jordan Creek were enriched with mercury and manganese, which probably were ultimately caused by past mining in that basin. Below Crooked Creek, elevated suspended sediment concentrations (142 mg/L), phosphorus concentrations (0.23 mg/L), and E. coli populations (370 most probable number per 100 milliliters) during the largest spring runoff event could be the result of inputs at the lower end of Jordan Valley and (or) inputs from Crooked Creek. The New Zealand Mud Snail, a highly competitive gastropod introduced to the Snake River in the 1980s, was collected just downstream from the Crooked Creek confluence.

Idaho;Nevada;Oregon↗
USGS2002

Ground-water quality in the central High Plains aquifer, Colorado, Kansas, New Mexico, Oklahoma, and Texas, 1999

A network of 74 randomly distributed domestic water-supply wells completed in the central High Plains aquifer was sampled and analyzed from April to August 1999 as part of the High Plains Regional Ground-Water Study conducted by the U. S. Geological Survey National Water-Quality Assessment Program to provide a broad-scale assessment of the ground-water-quality in this part of the High Plains aquifer. Water properties were relatively consistent across the aquifer, with water being alkaline and well oxidized. Water was mostly of the calcium and magnesium-bicarbonate type and very hard. Sulfate concentrations in water from three wells and chloride concentration in water from one well exceeded Secondary Maximum Contaminant Levels. Fluoride concentration was equal to the Maximum Contaminant Level in one sample. Nitrate concentrations was relatively small in most samples, with the median concentration of 2.3 milligrams per liter. Dissolved organic carbon concentration was relatively low, with a median concentration of 0.5 milligram per liter. The Maximum Contaminant Level set by the U.S. Environmental Protection Agency for nitrate as nitrogen of 10 milligrams per liter was exceeded by water samples from three wells. Most samples contained detectable concentrations of the trace elements aluminum, arsenic, barium, chromium, molybdenum, selenium, zinc, and uranium. Only a few samples had trace element concentrations exceeding Maximum Contaminant Levels. Fifty-five of the samples had radon concentrations exceeding the proposed Maximum Contaminant Level of 300 picocuries per liter. The greatest radon concentrations were detected where the Ogallala Formation overlies sandstones, shales and limestones of Triassic, Jurassic, or Cretaceous age. Volatile organic compounds were detected in 9 of 74 samples. Toluene was detected in eight of those nine samples. All volatile organic compound concentrations were substantially less than Maximum Contaminant Levels. Detections of toluene may have been artifacts of the sampling and analytical processes. Pesticides were detected in 18 of the 74 water samples. None of the pesticide concentrations exceeded Maximum Contaminant Levels. The most frequently detected pesticides were atrazine and its metabolite deethylatrazine, which were detected in water from 15 and 17 wells, respectively. Most of the samples with a detectable pesticide had at least two detectable pesticides. Six of the samples had more than two detectable pesticides. Tritium concentrations was greater than 0.5 tritium unit in 10 of 51 samples, indicating recent recharge to the aquifer. Twenty-one of the samples that had nitrate concentrations greater than 4.0 milligrams per liter were assumed to have components of recent recharge. Detection of volatile organic compounds was not associated with those indicators of recent recharge, with most of volatile organic compounds being detected in water from wells with small tritium and nitrate concentrations. Detection of pesticides was associated with greater tritium or nitrate concentrations, with 16 of the 18 wells producing water with pesticides also having tritium or nitrate concentrations indicating recent recharge.

Colorado, Kansas, New Mexico, Oklahoma, Texas↗
USGS1977

The Eutaw-McShan aquifer in Mississippi

This report, the fifth in a series of 'atlas-type' reports, summarizes the large amount of unpublished data available for the Eutlaw-McShan aquifer in Mississippi. The Eutaw-McShan aquifer, of Cretaceous age, consists of the interconnected irregular sand beds in the Eutaw and McShan Formations. The aquifer contains fresh water in an area of about 8,000 sq mi in northeastern Mississippi. Water produced from the aquifer by 59 water systems and several industries in 1975 averaged about 24 mgd. Water levels have declined about 200 feet below levels of the early 1900 's at Tupelo and West Point and it is estimated that the aquifer is developed to near its potential yield at those places. The aquifer is used extensively in areas where the dissolved-solids concentration of the water is more than 500 mg/liter and in some places where the concentration exceeds 1,000 mg/liter. The most common water-quality problems are excessive chloride and fluoride. (Woodard-USGS)

Mississippi↗
USGS1976

Maps showing ground-water conditions in the lower Big Chino Valley and Williamson Valley areas, Yavapai and Coconino Counties, Arizona--1975-76

Arizona is divided into 67 ground-water areas, and individual areas are selected for intensive data collection once every 6 years. The data collected in the lower Big Chino Valley and Williamson Valley areas are given on maps that show depth to water, well depth, and altitude of the water level, 1975-76; pumpage, 1950-74; and specific conductance, fluoride concentration, and irrigated area, 1974. Scale 1:125,000. (Woodard-USGS)

Water-Resources Investigations Report↗
USGS1976

Maps showing ground-water conditions in the San Simon area, Cochise and Graham Counties, Arizona, and in Hidalgo County, New Mexico — 1975

Arizona is divided into 67 ground-water areas, and individual areas are selected for intensive data collection once every 6 years. The data collected in the San Simon area are given on maps that show depth to water, well depth, and altitude of the water level, 1975; pumpage, 1915-74; and change in water level for 1964-75, hydrographs of the water level in selected wells, specific conductance, and fluoride concentration.

Arizona, New Mexico↗
USGS1978

Ground-water storage in the Johnson Valley area, San Bernardino County, California

The Mojave Water Agency includes several desert basins where ground water in storage is many times as great as the average annual recharge. The Johnson Valley area in San Bernardino County, Calif., was evaluated for (1) the quantity of ground water in storage, (2) the chemical quality of the ground water, and (3) the potential for storage of recharge water in the unsaturated zone. Johnson Valley contains about 250,000 acre-feet of water in storage, of which about half can be considered recoverable. About 250,000 acre-feet of void space in the unsaturated alluvium is available for storage of imported water, but not all of the recharged water could be recovered. The quality of the water in storage is satisfactory for public consumption, although water from some areas has high floride concentrations and should be mixed with water of low fluoride concentration.

California↗